A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17739019



Internal ID162685
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:2527829..2636084hg38UCSC Ensembl
chrX:2445870..2554125hg19UCSC Ensembl
CytobandXp22.33
Allele length
AssemblyAllele length
hg38108256
hg19108256
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5415892
Supporting Variants
Samples
Known GenesCD99P1, LINC00102, MIR6089-1, MIR6089-2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17739019
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000208203


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